|Publication number||US7262174 B2|
|Application number||US 10/143,536|
|Publication date||Aug 28, 2007|
|Filing date||May 9, 2002|
|Priority date||May 9, 2001|
|Also published as||US20040147465, US20060239974, WO2002091999A2, WO2002091999A3|
|Publication number||10143536, 143536, US 7262174 B2, US 7262174B2, US-B2-7262174, US7262174 B2, US7262174B2|
|Inventors||Xu-Rong Jiang, Choy-Pik Chiu, Calvin B. Harley|
|Original Assignee||Geron Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (33), Non-Patent Citations (37), Referenced by (19), Classifications (33), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application claims the priority benefit of U.S. provisional patent application No. 60/289,903, filed May 9, 2001, pending. The priority application is hereby incorporated herein by reference in its entirety.
This invention relates to the field of the cell biology of epidermal cells and the substratum, and enhancement of the properties of these tissues for purposes of therapy. The invention also relates to the enzyme telomerase reverse transcriptase, and its use in regulating telomerase length.
The worldwide chronic skin wound market, which includes diabetic foot ulcers, venous stasis ulcers and bedsores, is estimated to bear over $6 billion annually in treatment costs. The number of patients is about 12.5 million. The largest proportion is the venous stasis market, estimated at $3 billion annually, or 3.6 million patients. Venous leg ulcers are a type of chronic wound that affects up to 1 million people in the U.S., 90% of whom are over age 50. Skin lesions also present for medical treatment following accidents that involve abrasion or burning of the dermis.
Pharmaceuticals under development for managing these conditions include compositions that promote activity of endogenous cells at the site of the wound.
The family of keratinocyte growth factors has been implicated in the process of wound healing. Beer et al. (J. Investig. Dermatol. Symp. Proc. 5:34, 2000) showed that KGF is weakly expressed in healthy human skin, but strongly upregulated in dermal fibroblasts after skin injury. Binding to a transmembrane receptor on keratinocytes induces both proliferation and migration of the cells, and protects them from toxic effects of reactive oxygen species. Soler et al. (Wound Repair Regen. 7:172, 1999) characterized KGF-2 as a potential wound healing agent. It was found to increase both proliferation and migration of keratinocytes, and promote healing of human meshed skin explanted grafts and surgical excisions.
U.S. Pat. Nos. 5,814,605 and 5,965,530 provide pharmaceutical compositions comprising keratinocyte growth factor (KGF-1), for use in reducing hair loss. U.S. Pat. No. 6,077,602 relates to the sequence of keratinocyte growth factor 2 (KGF-2) and variants with enhanced activity and stability, for use in promoting wound healing. KGF-2 is currently being evaluated in clinical trials for treating injuries and skin disorders.
Other options that have been proposed for promoting activity in cells near the wound include the following. U.S. Pat. No. 5,718,897 outlines a method of enhancing migration and proliferation of keratinocytes in wound healing, by treating the wound with collagenase and a growth factor. U.S. Pat. No. 5,997,863 outlines a method of enhancing wound healing by administering enzymes that degrade glycosaminoglycans such as heparin or chondroitin sulfate in various combinations. Inada et al. (Am. J. Pathol. 157:1875, 2000) propose to facilitate wound healing by activating the transglutaminase-1 gene. Jaakkola et al. (Gene Ther. 7:1640, 2000) used adenovirus to deliver the gene for growth factor inducible element named “FIRE” into wound margin keratinocytes. U.S. Pat. No. 6,001,805 provides a method of enhancing wound healing by stimulating fibroblast and keratinocyte growth in vivo using amphipathic peptides. U.S. Pat. No. 6,191,110 outlines a method of enhancing wound healing by stimulating fibroblast and keratinocyte in vivo using amphipathic peptides of a particular sequence.
Other compositions for promoting wound healing including isolated cells and cell matrices derived from the subject being treated or a third-party donor, and adapted to provide protection of the wound while healing takes place.
U.S. Pat. No. 5,980,888 relates to a biomaterial designed for treating skin wounds, in which keratinocytes are attached to microcarrier beads of 50-500 microns in diameter. International Patent Publication WO 97/08295 outlines a reconstituted skin, comprising a dermal matrix inoculated with epithelial cells or their progenitors. U.S. Pat. No. 5,861,153 outlines a skin equivalent, comprising a support, isolated keratinocytes, and Langerhans' cells that have been activated by culturing with keratinocytes or growth factors. U.S. Pat. No. 5,580,781 reports a method for treating a skin defect by applying epidermal tissue comprising cultured outer root sheath cells. U.S. Pat. No. 6,110,208 outlines an artificial human skin comprising a support comprising a microperforated membrane upon which keratinocytes have been seeded, and an underlying tissue upon which fibroblasts have been seeded.
Genetically modified epithelial cells have been investigated in several contexts. U.S. Pat. Nos. 4,868,116, 4,980,286, and 5,698,436 relate to the introduction and expression of foreign genetic material in epithelial cells. International Patent Publication WO 97/23602 outlines techniques for obtaining human skin cell lines that have been immortalized with the SF40 large T antigen, or the E6/E7 gene of HPV16.
In 1998, Organogenesis received FDA marketing clearance for its full-thickness artificial skin product, Apligraf®, for treating venous stasis wounds. Like human skin, the product has two primary layers, an outer epidermal layer made of living human keratinocytes, the most common cell type of the human epidermis, and an inner dermal layer consisting of living human fibroblasts, the most common cell type in the human dermis. The human keratinocytes and fibroblasts used in its manufacture are derived from donor tissue. Apligraf® is currently approved for treating venous leg ulcers and diabetic foot ulcers.
The considerable complexity of the wound healing process is reviewed in Science magazine (P. Martin, Science 276:75, 1997). The article takes the view that normal adult wound repair is less like patching and more like regeneration. In view of the pervasive presence of skin lesions in our aging population, there is a compelling need for new modalities in wound healing.
This disclosure provides materials and methods for treating wounds. Some aspects of the invention relate to agents that activate degenerative epithelial cells to restore normal mobility, resist apoptosis, and increase their proliferative capacity. The agents increase telomerase activity in epithelial cells and other cells present near a wound site, promoting the cells to move to the site and restore an epithelial layer. Other aspects of the invention relate to compositions comprising epithelial cells in which telomerase activity has been increased, useful as grafts in the treatment of wounds.
One embodiment of the invention is a pharmaceutical composition comprising a vector encoding telomerase reverse transcriptase (TERT), or other agent that increases telomerase activity or expression, formulated for administration to a wound site or an epithelial surface, such as the skin. The agent may be provided in a suitable excipient, such as a cream or gel, which may contain a constituent that enhances penetration or resistance to proteases, or otherwise enhances or prolongs efficiency. The composition may cause transient TERT expression in cells at the wound site if it is an adenovirus or lipid vector, or permanent TERT expression in cells and their progeny if it is a retrovirus vector. Some of the many effects possible are that epithelial cells treated with the composition express certain levels of telomerase activity (as measured in a TRAP assay), the ability to migrate on a solid surface at a substantial rate, or secretion of factors or matrix materials that promote wound closing.
Another embodiment of the invention is a pharmaceutical composition comprising telomerized epithelial cells or fibroblasts. The composition may further comprise a microparticle or matrix to enhance administration to a wound site or an epithelial surface, such as the skin, and may be further accompanied by a matrix or dressing for attaching the cells to a treatment site. In certain circumstances, the telomerized cells in the composition may express certain levels of telomerase activity, or the ability to migrate on a solid surface at a substantial rate.
Other embodiments of the invention relate to treating a wound or an epithelial cell surface, using a pharmaceutical composition of this invention. Exemplary are compositions containing a vector encoding telomerase reverse transcriptase (TERT), or compositions containing telomerized epithelial cells. Included are methods in which an agent is applied that causes increased expression of TERT in cells at the wound site. Subsequently, the treatment site can be monitored for effect of the composition, such as closing of the wound or reepithelialization of the surface. Administering the composition may have a number of beneficial effects, such as enhancing wound closure compared with an untreated wound, increasing TERT activity or expression in any restorative cell type present in the wound.
Another embodiment of the invention is a method of increasing migration of an epithelial cell, comprising causing increased telomerase activity in the epithelial cell (for example, by causing increased expression of TERT in the cell). The cell may subsequently be monitored for the effect of treatment, such as telomerase activity, or the ability to migrate on a solid surface.
Another embodiment of the invention is a method for screening a compound for its ability to affect cell migration, epithelialization, or wound healing, either in vitro or in vivo. For example, the compound can be contacted with telomerized epithelial cells in culture, and the effect on migration can be determined. Alternatively, the compound can be administered to an epithelial surface comprising telomerized cells on a living subject, and the effect on the treated cells can be determined.
The pharmaceutical methods and treatment compositions can be used for any therapeutically desirable purpose, including the treatment of any epithelial surface for wounds or any other perceived imperfection. The invention is particularly suitable for treating acute lesions, such as a traumatic lesion, burn, or surgical incision; and chronic lesions, such as a chronic venous ulcer, diabetic ulcer, or compression ulcer.
Other aspects of the invention will be apparent from the description that follows.
Panel (a) shows results of the HEKn9 neonatal keratinocyte line transduced early in culture with the human TERT retrovirus vector, or with vector control (BABE). TERT expressing keratinocytes taken to 152 population doublings retained migration characteristics of very young cells (PD8), which is at least 3-fold higher than the migration rate usually observed in keratinocytes reaching their doubling limit (PD41).
Panel (b) shows results of old HEKn9 cells (PD41) transduced with adenovirus vector for transient expression of hTERT, or with vector control (AdGFP). Short-term induction of telomerase activity in these cells restored their ability to close the wound.
No TRAP activity was detectable in AdhTERT transduced tissues, presumably due to low efficiency of gene transfer or expression.
The Bottom Panel provides results of normal skin tissue, and skin taken near a chronic wound in the same donor (GTS 1388, age 39). Epidermal migration was slower in the wound. AdhTERT enhanced migration of the wound tissues by almost 3-fold, but had no effect on the normal tissue. The effect is greater than would be expected based on the number of cells detectably expressing hTERT, indicating that the transfected cells are recruiting activity in the surrounding epithelium.
The healing of an adult skin wound is a complex process, requiring collaboration between different cells and tissues. The phases of healing involve proliferation, migration, matrix synthesis, and contraction of the collaborating cells. Compositions that advance these processes may provide considerable improvement to the therapeutic modalities available.
It has now been discovered that increasing telomerase activity has a variety of effects that enhance the wound-healing potential of cells near the site of the wound. Replication is enhanced, and the cells become less susceptible to triggers of apoptosis. A surprising finding made in the course of this work is that telomerase expression also substantially enhances mobility of old cells surrounding the wound—allowing them to close the wound more rapidly. This is of considerable interest, because reepithelializing open areas of the wound creates a sterile barrier, and enhances healing of the subdermal tissues.
The enzyme telomerase is known to be generally involved in maintaining telomere length and forestalling replicative senescence in dividing cells. Most normal human somatic cells possess low or undetectable levels of telomerase, and their telomerase shorten with each cell division, ultimately leading to replicative senescence.
Kang et al. (Cell Growth Differ. 9:85, 1998) found that normal human oral keratinocytes (but not fibroblasts) have levels of telomerase measurable by telomeric repeat amplification protocol (TRAP) that diminished as the cells were passaged. Harle-Bachor et al. (Proc. Natl. Acad. Sci. USA 93:6476, 1996) dissected human skin taken during surgery, and tested for telomerase levels. They found that dermal fibroblasts were telomerase negative, but the epidermis had detectable telomerase activity, attributable to proliferative basal cells, which may act to promote regeneration of the epidermis. Fujimoto et al. (Oral. Oncol. 37:132, 2001) measured telomerase expression in oral keratinocytes and squamous cell carcinomas. Campisi et al. (J. Invest. Dermatol. 3: 1, 1998) and Mendez et al. (J. Vasc. Surg. 28:876, 1998) reported that loss of telomerase, proliferative capacity, and function are associated with skin aging and chronic wounds.
Artificially increasing the expression of telomerase can prevent the onset of senescence in some normal cells, increasing replicative capacity without causing malignant transformation (Bodnar et al., Science 279:349,1998; Yang et al., J. Biol. Chem. 274:26141, 1999; Morales et al., Nature Genet. 21:115, 1999). Ectopic expression of telomerase has been found to immortalize skin fibroblasts and microvascular endothelial cells, while maintaining growth control and differentiated function (Jiang et al., Nature Genet. 21:111, 1999). Farwell et al. (Am. J. Pathol. 156:1537, 2000) determined genetic and epigenetic changes in epithelial cells immortalized by telomerase. Yang et al. (Nat. Biotechnol. 19:219, 2001) determined the effect of telomerase on human microvasculature in vivo. Funk et al. (Exp. Cell Res. 258:270, 2000) found that telomerase expression restores dermal integrity to in vitro aged fibroblasts in a reconstituted skin model.
However, before the filing of the present disclosure with the Patent Office, previous reports of epithelial cells with increased telomerase expression have taught against the invention claimed in this application. It has been reported that telomerase expression is insufficient to immortalize keratinocytes. Loss of cell cycle control was believed to be a second requirement for immortalization—specifically, inactivation of the pRb/p16INK4a pathway (Dickson et al., Mol. Cell. Biol. 20:1436, 2000; and Kiyono et al. Nature 396:84, 1998).
In spite of those discouraging reports, the experiments detailed below were conducted to determine what effect increased telomerase activity in keratinocytes would have on phenotypic features of the cells. Ectopic telomerase expression by itself was found to be sufficient for primary keratinocytes to bypass senescence and extend their life span—even in the absence of Rb/p16INK4a cell cycle control disruption. Normal levels of c-myc protooncogene expression, and normal growth and differentiation are maintained (Example 2, below). Furthermore, keratinocyte cultures established from adult donors and subsequently telomerized were shown to lose their susceptibility to apoptosis-inducing agents (Example 4).
A significant aspect of this discovery in the context of wound healing is that upon telomerization, epithelial cells from older adults acquire considerably improved capacity to mobilize and move into open areas of a wound. As shown in
Another remarkable finding during the course of this investigation is the ability of telomerized cells to recruit activity of other cells to promote wound closure.
The description that follows illustrates how this discovery can be implemented in clinical therapy in a variety of embodiments. Polynucleotide vectors and other agents can be applied to increase telomerase expression in cells around the site of a wound, thereby initiating or enhancing reepithelialization and closure of the wound over underlying tissues. Alternatively or in addition, the wound can be treated with a preparation of telomerized cells to overlay or repopulate the open area of a wound. These strategies can be implemented as effective treatments on their own, and can also be used as effective adjuncts to other wound-closing therapies.
For further elaboration of general techniques useful in the practice of this invention, the practitioner can refer to standard textbooks and reviews in cell and molecular biology, tissue culture, and veterinary and human medicine.
Methods in molecular genetics and genetic engineering are described generally in the current editions of Molecular Cloning: A Laboratory Manual, (Sambrook et al., Cold Spring Harbor); Gene Transfer Vectors for Mammalian Cells (Miller & Calos eds.); and Current Protocols in Molecular Biology (F. M. Ausubel et al. eds., Wiley & Sons). Cell biology, protein chemistry, and antibody techniques can be found in Current Protocols in Protein Science (J. E. Colligan et al. eds., Wiley & Sons); Current Protocols in Cell Biology (J. S. Bonifacino et al., Wiley & Sons) and Current protocols in Immunology (J. E. Colligan et al. eds., Wiley & Sons.). Reagents, cloning vectors, and kits for genetic manipulation referred to in this disclosure are available from commercial vendors such as BioRad, Stratagene, Invitrogen, and Clontech.
Cell culture methods are described generally in the current edition of Culture of Animal Cells: A Manual of Basic Technique (R. I. Freshney ed., Wiley & Sons); Culture of Epithelial Cells (R. I. Freshney ed., Wiley & Sons), General Techniques of Cell Culture (M. A. Harrison & I. F. Rae, Cambridge Univ. Press).
Topical publications include Molecular Biology of the Skin: The Keratinocyte (M. Darmon & M. Blumenberg, eds., Academic Press), Wound Closure Biomaterials and Devices (Chu et al. eds., CRC Press), and Biomembranes Part V: Cellular and Subcellular Transport: Epithelial Cells (S. Fleischer & B. Fleischer eds., Meth. Enzymol. vol. 191).
Skin cells and epithelial cells of various types can be isolated from tissue samples taken from humans and other species to validate the effectiveness of agents proposed for increasing telomerase levels, and to prepare some of the telomerized cell compositions of this invention.
Primary cultures of keratinocytes (skin epithelial cells) are readily obtained by culturing skin cells that have been separated by dissection and/or enzymatic digestion from a corresponding sample of epithelium, such as split-thickness explants of human skin. The cells can be passaged in serum-free medium, and form confluent, stratified cultures.
In one method, a layer of feeder cells is prepared form the 3T3 line of human fibroblasts (ATCC Accession No. CRL-1658). The feeders are grown in 3T3 medium at 37° C. to ˜50% confluence, treated with mitomycin c (1-10 μg/mL) for 12 h, and then seeded at 2.5×104 cells/cm in keratinocyte growth medium (KGM: DMEM/F12 1:3, 10% fetal calf serum, 4 mM L-glutamine, 100 U/mL penicillin & streptomycin, 0.4 μg/mL hydrocortisone, cholera endotoxin (1×10−10 M), transferrin (5 μg/mL), liothyronine (2×10−11 M), adenine (1.8×10−4 M), insulin (5 μg/mL) and EGF (10 μg/mL). A skin sample is submerged briefly in alcohol 3 times, dried, and trimmed to remove hypodermis so only the epidermis and relatively dense dermis remain. The sample is then cut into 2-3 mm thin strips, and covered with medium containing dispase at 2 mg/mL overnight at 4° C., or for 2-4 h at 37° C. The epidermis is then peeled away from the dermis using two sterile hypodermic needles, and placed into 5 mL 0.05% trypsin solution with shaking for 1 min. Fifteen mL DMEM containing 10% FCS is added to inactivate the trypsin, and pieces of the upper epidermal layer is removed by passing through sterile gauze. The flow-through single-cell suspension is then centrifuged at 300 g for 5 min, resuspended in KGM, and plated on to the feeder layers at 2-5×104 viable cells cm−2, or onto a collagen-IV coated flask.
Other methods for culturing keratinocytes are described by Rheinwald and Green (Cell 6:331, 1976), Flaxman et al. (Br. J. Dermatol. 92:305, 1975), Price et al. (J. Natl. Cancer Inst. 70:853, 1983), Wilke et al. (J. Natl. Cancer Inst. 80:1299, 1988), Germain et al. (Burns 19:99, 1993); and reviewed by Daniels et al. (Burns 22:35, 1996) and Barlow et al. (Methods Mol. Biol. 75:117, 1997). U.S. Pat. No. 5,712,163 provides chemically defined culture media for culturing epithelial cells, containing nutrients, insulin or IGF, transferrin or Fe2+, T3 or thyroxin, an ethanolamine, and calcium above 1.0 mM. Depending on the source and the culture method, doubling times can be achieved of up to 33 hours, and between 20 and 50 population doublings. Telomerase activity in the cultured epithelial cells can then be increased as described in the following section. U.S. Pat. No. 4,016,036 provides a process for serially culturing keratinocytes on a layer of inactivated fibroblast feeder cells. As an alternative, the cells can be grown on a porous analog of the extracellular matrix that supports the cells in vivo, such as collagen (Orgill et al., J. Biomed. Mater. Res. 15:39, 1998).
As an alternative, useful cell populations can be obtained by providing a population of stem cells, and then permitting or causing the cells to proliferate or differentiate into the desired phenotype. Li et al. (Proc. Natl. Acad. Sci. USA 31:3902, 1998) isolated and characterized candidate human keratinocyte stem cells. U.S. Pat. No. 6,200,806 (Thomson) and U.S. Pat. No. 6,090,622 (Gearhart et al.), and International Patent Publication WO 99/20741 (Geron Corporation) provide compositions of human pluripotent stem cells.
Tani et al. (Proc. Nati. Acad. Sci. USA 97:10960, 2000) provide enrichment methods for keratinocyte stem cells based on cell surface phenotype. Jones et al. (Cell 73:713, 1993) and International Patent Publication WO 99/47644 report enrichment of human keratinocyte stem cells to a high degree of purity using cell-surface integrins. Pellegrini et al. (Med. Biol. Eng. Comput. 36:778, 1998) provide cultivation conditions for human keratinocyte stem cells. Bata-Csorgo et al. (J. Clin. Invest. 95:317, 1995) report kinetics and regulation of human keratinocyte stem cell growth in short-term primary ex vivo culture.
Differentiation into a phenotype characteristic of certain types of epithelial cells can be determined according to characteristic morphology and cell-surface markers, such as cytokeratins (K1, K4, K10), integrins (integrin β1, α6β4 integrin), and the receptor for keratinocyte growth factor. Stem cells differentiated to the desired phenotype can then be treated to increase the level of telomerase activity. Alternatively, the stem cell can be genetically altered to increase telomerase activity in cell progeny, and then differentiated into an epithelial cell with appropriate characteristics.
The compositions and techniques of this invention are generally applicable to different types of cells at the site of a wound, including but not limited to epithelial cells such as keratinocytes, and the underlying substrata. Reference to keratinocytes in the following description serves as a model for other types of cells, and is not meant to limit the practice of the invention except where explicitly required. Cells suitable for treatment in accordance with this invention include epithelial cells of the dermis, and of the internal mucosa. Clinical aspects of this invention can be performed on human patients, and veterinary subjects such as pets, livestock, other mammals, avians, and other vertebrates, as appropriate.
Other cells of interest in the practice of this invention can be studied in situ or isolated according to any suitable technique. For example, isolation and culture of human fibroblasts is described inter alia by Houck, Sharma & Hayflick, Proc. Soc. Exp. Biol. Med. 137:331, 1971; and in U.S. Pat. Nos. 5,460,959 and 6,093,393. Fibroblasts can be recognized by their characteristic stellate or spindle shape, ability to form collagen, or ability to respond to fibroblast growth factors (FGF). Gupta et al. (Exp. Cell Res. 230:244, 1997) and Cha et al. (Yonsei Med. J. 37:186, 1996) describe techniques for isolation and culture of human dermal microvascular endothelial cells. Isolation, characterization, and culture of mucosal epithelial cells are described by Pool-Zobel et al., Environ. Mol. Mutagen. 24:23, 1994; and in International Patent Publication WO 00/03002.
Increasing Telomerase Activity
Increasing telomerase activity in cells according to this invention can be accomplished by any effective mechanism, including but not limited to the following:
A convenient method to increase telomerase activity is to genetically alter the cells so that they express TERT, which is the limiting component of telomerase enzyme expression in most cells. A TERT gene can be cotransfected with a gene for the telomerase RNA component, or a TERT can be selected that is compatible with the RNA component already expressed by the cell. A cell is referred to in this disclosure as “telomerized”, if it has been genetically altered with a recombinant polynucleotide to increase functional telomerase activity, either on a transient or permanent basis.
The polynucleotide and amino acid sequence of human TERT is provided in SEQ. ID NOs:1 & 2. See also Nakamura et al., Science 277:955, 199; and U.S. Pat. Nos. 6,166,178 and 6,261,836, which describe the use of TERT to increase replicative capacity of various cell types. Vectors used to express human TERT typically encode at least 10, 30, or 100 consecutive amino acids in SEQ. ID NO:2, or a protein sequence that is at least 70% or 90% identical to a fragment of SEQ. ID NO:2, and having telomerase reverse transcriptase activity. The encoding sequence typically encodes at least 25, 100, or 300 consecutive nucleotides in SEQ. ID NO:1, or a nucleotide sequence 70% or 90% identical to a fragment of SEQ. ID NO:1, or hybridizes to such a sequence under stringent conditions.
When TERT is referred to in this description, it is understood to mean a polypeptide comprising a TERT sequence from any species, with or without alterations (such as insertions, mutations and deletions) with respect to the native sequence—so long as the gene product has telomerase catalytic activity when associated with telomerase RNA component, as measured by TRAP assay, described below. Mouse TERT sequence is provided in International Patent Publication WO 99/27113. Other publications with telomerase-related sequences include International Patent Publication WO 98/21343 (Amgen); WO 98/37181 (Whitehead); WO 98/07838A1 (Mitsubishi); WO 99/01560 (Cambia), and U.S. Pat. No. 5,583,016 (Geron Corp.). U.S. Pat. Nos. 5,968,506 and 6,261,556 (Geron Corp.) describes purified mammalian telomerase and methods for obtaining it.
Expression vectors embodied in this invention are polynucleotides that have an encoding region, which upon expression in a target cell, is able to confer on that cell an increase in telomerase activity. Typically, vectors with a TERT encoding sequence will further comprise a heterologous transcription control element that will promote transcription in the intended undifferentiated or differentiated cell line. Sequences that can drive expression of the TERT coding region include viral LTRs, enhancers, and viral promoters (such as MPSV, SV40, MoLV, CMV, MSCV, HSV TK), eukaryotic promoters (such as β-actin, ubiquitin, elongation factors exemplified by Ef1α, ubiquitin, and PGK) or combinations thereof (for example, the CMV enhancer combined with the actin promoter).
A TERT expression cassette can be delivered into the cell genome using a suitable vector system, such as a retrovirus or adenovirus. Transfection and expression of telomerase in human cells is described in Bodnar et al., Science 279:349, 1998 and Jiang et al., Nat. Genet. 21:111, 1999. For causing TERT expression on a permanent basis (for example, to create telomerized cells for administration), the pBABE retroviral vector shown in
As an alternative, the replicative capacity of the cell line can be enhanced without integrating a TERT gene into the genome. For example, TERT can be transiently expressed using a suitable expression system such as adenovirus, or by introducing TERT protein (or the telomerase holoenzyme) directly into the cell. The TERT will be diluted out as the cell divides, but extension of telomerase in the parent cell should increase replicative capacity of the cell line by several doublings. Other suitable vectors include nucleic acid-lipid compositions effective for causing expression of the encoded protein, such as DNA lipofectin or lipofectamine complexes, neutral or anionic liposomes (U.S. Pat. Nos. 5,753,258, 5,756,122, 5,981,501), cationic lipid complexes (U.S. Pat. Nos. 6,008,202, 6,020,202 and 6,071,533), or combinations with amphipathic lipids (WO 00/59474).
Another alternative is to upregulate TERT expression from the endogenous gene by upregulating expression of trans-activating transcriptional regulators. The TERT promoter contains a number of regulator recognition sequences, such as c-myc, SP1, SRY, HNF-3β, HNF-5, TFIID-MBP, E2F and c-myb. See International Patent Publication WO 00/46355.
Another alternative is to deliver to the cell an enzyme capable of conferring telomerase activity. For example, telomerase can be purified by affinity techniques from cells that express the holoenzyme (U.S. Pat. No. 6,261,556). Telomerase reverse transcriptase (or an enzymatically active fragment) can be combined with telomerase RNA component (U.S. Pat. No. 5,837,857) either in solution or by cotranslation in a manner that permits reassembly into a telomerase holoenzyme. The active enzyme is then provided in a form that permits it to be translocated across the cell membrane (U.S. Pat. No. 5,059,532; WO 97/04748).
A further alternative is not to increase TERT expression, but enhance the effective activity of telomerase already present in the cell. This is effective in cells that have an endogenous level of TERT expression, such as in bone marrow progenitor cells and gonadal tissue. For example, TRF1 and TRF2 are proteins that bind to telomere repeats and regulate access of telomerase (Smogorzewska et al., Mol. Cell Biol. 20:1659, 2000). Decreasing expression of such factors may enhance the ability of telomerase to increase telomere length, thereby increasing replicative capacity of the cell. Furthermore, the presence of phosphatase inhibitors or protein kinase activators has been reported to increase telomerase activity (Li et al., J. Biol. Chem. 272:16729, 1998; Bodnar et al., Exp. Cell Res. 228:58, 1996).
Determining Telomerase Activity and the Effect on Cell Behavior
Evidence of increased telomerase expression can be obtained by a variety of techniques, including but not limited to determining gene transcript levels (for example, by Northern or RT-PCR analysis), protein expression (for example, by immunocytochemistry), or telomerase activity (for example, by primer extension assay). Extended lifespan or replicative capacity of the treated cells, while often desirable, need not be positively demonstrated for the invention to be put into practice, except where explicitly required.
Telomerase activity can be determined by TRAP assay (Kim et al., Science 266:2011, 1997; Weinrich et al., Nature Genetics 17:498, 1997), or other suitable technique (e.g., U.S. Pat. No. 5,741,677). Desirable levels of telomerase activity are at least 1, 4, 10, or 20 TPG units, calculated as described in Example 2. Evaluation of TERT expression by RT-PCR or immunoassay can be done by standard methods, using the sequences disclosed in U.S. Pat. No. 6,166,178. Absent of evidence to the contrary, it can be assumed that elevated levels of TERT transcript or protein corresponding to telomerase reverse transcriptase is an indication that the activity of telomerase in the cell is also elevated. The following assay kits are available commercially for research purposes: TRAPeze® XL Telomerase Detection Kit (Cat. s7707; Intergen Co., Purchase N.Y.); TeloTAGGG® Telomerase PCR ELISApIus (Cat. 2,013,89; Roche Diagnostics, Indianapolis Ind.); and LightCycler TeloTAGGG® human TERT quantification kit (Cat. 3,012,344).
Migration of isolated epithelial cells can be determined by plating or culturing in a monolayer, creating an adjacent free space on the substrate, and periodically observing cells moving into the free space. The migration occurs even in the absence of chemotactic factors, although the response of the cells to such factors may be of interest. The assay can also include a replication inhibitor such as mitomycin c, to decouple migration from cell replication. In a preferred method (Example 3), keratinocytes are grown as a monolayer on a standard tissue culture surface (such as a T25 flask) in regular medium until ˜80-90% confluent. A transverse area is then cleared by scraping, and migration of the cells into the cleared area is observed as a function of time. Depending on other features of the cell, migration of telomerized epithelial cells can be 1, 2, 5, or 10 cell diameters per day; or 2, 3, or 5-fold higher than cells of the same type that are untreated or treated with a control vector.
Effectiveness of compositions of this invention in closing or reepithelializing a wound can be ascertained in a suitable model. Since hTERT affects telomerase activity in non-human primates and other mammals, preclinical development is well suited to animal testing. A number of established animal models are available. Jimenez et al. (J. Surg. Res. 81:238, 1999) measured the effect of KGF-2 in linear incisions made in dorsal skin of rats. Cribbs et al. (J. Burn Care Rehabil. 19:95, 1998) tested the wound healing effect of heparin-binding EGF-like growth factor in an animal burn model. Leivo et al. (Br. J. Dermatol. 143:991, 2000) measured reepithelialization rate and protein expression in a human suction-induced wound model.
Human skin can also be transplanted onto the nude mouse for evaluating wound healing in a superficial excisional full-thickness wound. See for example Rossio-Pasquier et al., Arch. Dermatol. Res. 291:591, 1999. Epidermal wound healing can also be characterized using human skin specimens in an organ culture model. Moll et al. (J. Invest. Dermatol. 111:251, 1998) found that dissociated autologous keratinocytes promoted reepithelialization of 3 mm diameter defects made in excised skin specimens.
Repopulation of human keratinocytes and fibroblasts can be tested in a spontaneous cell sorting model. See Funk et al., Exp. Cell Res. 258:270, 2000; and Wang et al., J. Invest. Dermatol. 114:674, 2000. Two-piece silicon chambers (Renner, Germany) are surgically implanted onto the backs of SCID mice to provide an aseptic wound bed resting on the muscle fascia. Dermal fibroblasts and keratinocytes are harvested from culture and resuspended in serum-free medium. Human skin reconstitutions are initiated by placing a slurry of 6×106 keratinocytes and 6-8×106 fibroblasts (isolated as already described, or obtained from an established cell line such as BJ fibroblasts). After one week, the upper chambers are removed to allow aeration of the skin surface. The skin can then be tested for blister resistance or examined microscopically.
A full-thickness human skin xenograft model can be set up using skin samples from tissue bank or surgical discards from hospitals. The samples are trimmed of subcutaneous fat tissue and cut into pieces of 1-2 cm2. SCID mice are anesthetized using isofluorane, and 0.1 mL buprinex is administered s.c. (0.1 ml) behind the nape of neck as analgesic. A full thickness skin bed matching the size of the skin graft is created on the shaved dorsal region of the animal where there is a larger surface area and better vascular supply. One or two grafts are sutured in place using 4-0 Dermalon™ (Sherwood Davis & Geck) or 6-0 Vicryl™ (Ethicon). Any bleeding is stopped by applying gelfoam™. Petroleum jelly and telfa pad is applied, and the area bandaged using elastikon™ and conform™. The bandage and the sutures are removed 14 days later, with one change of bandage at 7 days. Scabbing ensues, and the grafts can be tested after the scabs come off, usually between 4-12 weeks.
The skin structure of the xenografts is monitored by immunohistochemistry using antibodies for human skin associated markers such as involucrin (NeoMarkers), associated with upper layers of the stratum corneum and the epidermis; collagen IV (Sigma), associated with the basal portion of the epidermis; and collagen I (Southern Biotech), associated with the dermal component. These antibodies are human-specific, and do not cross-react with murine skin. In general, the xenografts are positive for all three markers with some variability. The level of murine invasion can be determined using antibodies against human vs. mouse MHC Class I antigen. The amount of mouse cell invasion is variable from graft to graft, and increases with time post-surgery.
To monitor wound healing in the xenograft model, a 3 or 4 mm wound is created in the center of the skin xenograft using a sterile biopsy punch. Bleeding can be stopped using hemostatic sponges, and an occlusive bandage is placed on top of the wound for 2 days. Immediately before bandaging and every other day after bandage removal, the size of the wound is traced using an extra fine Sharpie® pen onto a clear, sterile Hybridwell™ strip until the wound is completely closed. Most of the wounds achieve complete closure by about 2 weeks. The size of the wound is quantified with respect to time by scanning each strip into ImageQuant™ or Photoshop™ 5.03, and performing area integration of the wound outlines with Openlab™ 2.1 or lmageQuant™. Using the best curve fit function, time to 50% and 75% wound closure is determined.
One way to determine the effect of increased telomerase expression is to deliver AdhTERT or control virus to the biopsy wound by direct intra-dermal injection, topical application, or both. For example, 1×107 to 5×108 particles are resuspended in 50 μL viral dilution buffer (saline +10% glycerol), and 10-15 μL aliquots are injected into 4 different sites i.d. using a tuberculin syringe with a 29 gauge needle. Alternatively, the virus is resuspended in 20 μL and directly applied to the wound bed. After allowing 30 minutes absorption and diffusion, the wound is bandaged using Opsite™ IV (Smith & Nephew) for 2-3 days. The kinetics of wound healing is then monitored as already described. The skin xenografts are harvested at different times following wounding for analysis of skin associated markers and telomerase expression.
Systems for testing telomerase activating agents and telomerized cells in tissue culture and animal models are illustrated below in Examples 2-8
The techniques and compositions provided in this disclosure can be used for a variety of desirable purposes. Such purposes include research or investigational work related to the behavior of epithelial cells or cells expressing telomerase. Of particular interest is clinical use in human or veterinary medicine, such as for the treatment of wounds or enhancement of properties of the dermis wherever desired.
Compositions for clinical use according to this invention include two categories: agents that can be used to increase telomerase activity in cells already present at or around an area of the epithelium in need of treatment; and compositions containing cells with increased telomerase activity. In general, such compositions are effective in treating a wound or otherwise enhancing properties of an epithelial surface in the body when applied individually, but they may also be used in combination where the benefits of both are desired.
Agents that Increase Telomerase Activity
Agents of this invention designed to increase telomerase activity or expression include vectors encoding TERT, agents that increase transcription of the endogenous TERT gene, and agents that affect the TERT gene product, transactivators or telomerase associated proteins in a manner that increases telomerase activity in cells near the wound that is being treated.
Compositions of this invention can be formulated for treating wounds of the skin or dermis, with or without involvement of the substratum and the underlying tissues. Compositions of this invention can also be formulated for treating wounds of other epidermal surfaces, including mucosal surfaces such as the bronchus, mouth, nose, esophagus, stomach, or intestine. Unless specifically required otherwise, the techniques and compositions of this embodiment are generally applicable to humans and other vertebrates.
Suitable TERT vectors include viral vectors, naked DNA, and DNA-liposome complexes, in which the TERT encoding region is operatively linked to transcription and translation elements active in the target cell. These vectors may include a constitutive promoter (such as the CMV or EF1α promoter), or a tissue-specific promoter (such as promoters for cytokeratins or integrins expressed in epithelial cells, or the receptor for keratinocyte growth factor).
When this disclosure refers to administration of an agent “to a wound site”, what is meant is that the agent is placed at, in, or around the wound in one or more locations, such that cells at the site of administration are caused to express increased telomerase activity or increased expression of TERT. The type of cells that may be affected include epithelial cells, keratinocytes, microvascular cells, and other cells subjacent to the affected surface or exposed during wounding. It is understood that most agents of this invention administered with a view to increasing telomerase activity in a particular cell type, such as an epithelial cell, will inevitably also affect other cell types in the vicinity. Evidence of telomerase expression or clinical benefit in the general area of the wound is a desired object, and it is not necessary to understand the effect on a particular cell type at the treatment site in order to practice the invention.
The therapeutic composition will contain an amount of the agent effective for accomplishing one, two or more than two of the following effects: a) increase in the level of telomerase activity or TERT expression in epithelial cells at the treatment site; b) increase in the level of telomerase activity or TERT expression in fibroblasts or other cells at the treatment site; c) increase the mobility of epithelial cells on a solid surface (as determined in an in vitro assay); d) cause reepithelialization of a wound or epithelial surface; and e) increase the rate of wound closure or healing as determined by clinical criteria. These effects may be obtained in a single dose, or by sequential administration of two or more doses after an appropriate interval. The amount given per dose depends on the efficiency of the agent or vector chosen. For example, retroviral vectors are typically used at a titer of about 106 to 107 per mL, adjusted empirically.
General aspects of formulation and administration of pharmaceutical compounds can be found in the latest edition of Remington's Pharmaceutical Sciences (Maack Publishing Co, Easton Pa.). With respect to the use of nucleic acid vectors in therapeutic applications, the reader may wish to consult The Skin and Gene Therapy (U. R. Hengge & B. Volc-Platzer eds., Springer Verlag, 2000), or Gene Therapy (Advances in Pharmacology, Vol 40) (J. T. August, J. Coyle & M. W. Anders eds., Academic Press 1997).
The agent may be administered in an excipient suitable for topical administration, or administration to a wound site. This means that the excipient will have one or more of the following three properties: a) enhanced ability to penetrate the dermis or tissues at the wound site (compared with a neutral isotonic solvent); b) enhanced ability for keeping the agent at the site long enough to enhance the effect; or c) ability to prolong activity of the agent when administered to the dermis or the wound site. Excipients that enhance penetration contain organic solvents or additives such as alcohol, oils, glycols, and emoluments, or specific carriers that cause binding to the target cell. Excipients that keep the agent at the target site include creams, gels, and semisolid compositions, or solutes that produce a semisolid or high viscosity medium once applied. Excipients that prolong longevity of the agent after administration depend on the nature of the effective agent. For example, protein or virus compositions will persist longer on the skin or at a wound site if it is prepared in an excipient that contains protease inhibitors, such as metal chelators that inhibit metalloproteinase. Similarly, bare nucleic acid compositions will persist longer in an excipient that contains nuclease inhibitors. If helpful in enhancing the shelf life, the composition may be distributed in separate components to be combined just before administration.
The agent may alternatively or in addition be administered in a device suitable for topical administration, or administration to a wound site. Typically, the device will have the characteristic of either enhancing penetration or keeping the agent at the site long enough to enhance the effect. Devices of this nature include solid matrixes made of collagen, laminin, or other biocompatible polymers, and standard dressings (such as pads or bandages) made of gauze, nylon, or various plastics. The device is typically adapted to stay in place at the site of treatment by conforming to the shape of the site, and having fasteners or positions for accommodating fasteners that allow it to be attached to the site. The product may be distributed as a combined composition, in which the device is impregnated with the agent, and designed to deliver the agent upon attachment. Alternatively, the product may be distributed as a kit, comprising the therapeutically effective agent, and a device for preparing the treatment site, or for applying the agent to the treatment site, or for covering the site during or after treatment (such as a suitable dressing).
At the option of the manufacturer or distributor, the pharmaceutical composition may be packaged with (or marketed using) a written indication for use of the product in treating wounds or the epithelium according to the invention.
Telomerized Cell Compositions
Isolated cells with increased telomerase expression or activity can be assembled into a therapeutic composition in several different forms. Generally, the composition will contain telomerized epithelial and/or fibroblast cells matched to the species and type of wound being treated: for example, keratinocytes and fibroblasts for skin lesions; mucosal epithelial cells for lesions to the gastrointestinal tract. The cells may further be engineered to express other factors that promote wound healing, such as growth factors or cytokines (e.g., KGF or FGF).
In one embodiment, telomerized epithelial cells are prepared as a suspension in a pharmaceutically compatible excipient, such as a buffer or semi-solid gel. Siedler et al. (Arch. Dermatol. 136:676, 2000) propose human fibrin glue containing keratinocytes for healing of chronic ulcers. The epithelial cells are optionally accompanied by other cells that facilitate engraftment or support the cells after engraftment, such as fibroblasts, endothelial cells, or Langerhans cells, which may or may not be telomerized.
In another embodiment, the cells are attached to a solid carrier from which they can migrate once applied to the wound. Suitable carriers include microcarriers (particles of any shape less than 1000 microns in diameter, with particles in the 100 micron range being preferred), and made of a compatible matrix such as collagen. See Voigt et al. (Tissue Eng. 5:563, 1999) and LaFrance et al. (Tissue Eng. 5:153, 1999). The large surface-to-volume ratio of the microspheres can provide a vehicle for delivering appropriate cell numbers while minimizing the amount of biomaterial to be absorbed. The composition is then applied directly to the wound cavity or ulcer, or to the region surrounding the wound from which the cells can migrate.
In another embodiment, the cells are provided in the form of a flat sheet. This may be advantageous for providing more immediate protection, or treating areas that have a paucity of proliferation-competent endogenous epithelial cells. In general, the sheet will comprise a two-dimensional arrangement of epithelial cells, supported in some manner by a porous matrix produced by other cells, or manufactured artificially using a biocompatible polymer (such as collagen, laminin, or other matrix proteins). The epithelial cells may in some cases be underlaid by a supportive layer of cells such as fibroblasts that enhance engraftment or shelf life. In accordance with this invention, cells in the composition can be either telomerized before forming into sheets, or the sheet can be preformed ex vivo (or isolated from a donor), and then telomerized using one of the vectors described earlier. If fibroblasts are contained in the composition, they may also be telomerized. The sheet is then prepared for transport, and grafted onto the wound site in the clinic.
U.S. Pat. No. 4,304,866 describes a method of producing transplantable sheets by culturing keratinocytes in a vessel and then detaching a sheet of cells from the vessel with a neutral protease such as dispase. U.S. Pat. No. 5,759,830 provides a three-dimensional fibrous scaffold containing attached cells for producing vascularized tissue in vivo. Orgill et al. (J. Biomed. Mater. Res. 39:531, 1998) outline the use of island grafts of artificial skin, comprising keratinocytes and a copolymer of collagen and chondroitin sulfate. International Patent Publication WO 99/63051 outlines a bioengineered flat sheet graft prosthesis comprising layers of processed tissue material.
When this disclosure refers to administration of a cell composition “to a wound site”, what is meant is that the composition is placed over, in, or around the wound, so as to provide coverage of at least part of the wound, or create a site from which the administered cells can migrate into the wound and promote closure or healing.
The cell compositions of this invention intended for clinical or veterinary use can be provided in an isotonic excipient, prepared under sufficiently sterile conditions for administration to the subject. They are optionally provided on a microparticle or matrix suitable for topical administration or administration to a wound site. This means that the microparticle or matrix is either adapted to adhere to the site of administration (using fasteners or dressing, if needed); or that the microparticle or matrix provides a vehicle from which the cells can migrate into the treatment site and participate in coverage of the site, reepithelialization, or healing.
Duration of the graft cells at the treatment site may be temporary or permanent, depending on the nature of the condition being treated and concurrent therapies. For permanent engraftment, it may be desirable to use compositions in which the cells are autologous or histocompatible with the patient being treated, although this is not always required. The product may be packaged as a single composition suitable for immediate use, or it may be packaged as a kit with component parts in separate containers to be admixed before administration, or for sequential administration. The kit may also contain a dressing or other substance for covering the site or improving engraftment. At the option of the manufacturer or distributor, the pharmaceutical composition may be packaged with (or marketed using) a written indication for use of the product in treating wounds or the epithelium wherever needed.
Conditions Suitable for Treatment
The techniques and compositions of this invention may be used for the treatment of wounds or other conditions of the epidermis wherever desired.
Some of the medical conditions that can be treated according to this invention are acute conditions (such as lesions suffered in trauma, burns, abrasions, surgical incisions, donor graft sites, and lesions caused by infectious agents). Other medical conditions that can be treated are chronic conditions (such as chronic venous ulcer, diabetic ulcer, compression ulcer, pressure sores, and ulcers or sores of the mucosal surface). Included are skin or epithelial surface lesions caused by a persistent inflammatory condition or infection, or by a genetic defect (such as keloid formation and coagulation abnormalities). This invention also contemplates manipulation of the skin and repair of any perceived defects in the skin surface for other purposes, such as cosmetic enhancement.
In the usual course of therapy, the treatment site is monitored for response to treatment. Desirable effects for agents that increase telomerase expression or activity include cell proliferation or migration at the treatment site, epithelialization of the surface, closure of a wound if present, or restoration of normal physiological function. Throughout this disclosure, “epithelialization” or “reepithelialization” of a treatment site means that the site acquires an increased density of epithelial cells as a result of the therapy that is applied.
Desirable effects for cell compositions include coverage of the treatment site, survival of the engrafted cells, lack of immune rejection, closure of the wound if present, or restoration of normal physiological function. The engrafted cells may participate in wound closure either by participating directly in the healing process (for example, becoming part of the healed tissue), or by covering the wound and thereby providing an environment that promotes healing by host cells.
Ultimate choice of the treatment protocol, dose, and monitoring is the responsibility of the managing clinician.
Other Uses of the Invention
Isolated cells, compositions, and mixed cell populations of this invention can also be used for any other desirable research, developmental, or therapeutic purpose. The high proliferative capacity and high mobility of telomerized epithelial cells can be maintained as the cells are passaged in culture, thereby providing a standardized reservoir of cells for further investigation. Cell cultures or matrixes can be combined with a putative therapeutic or cosmetic agent, and any alteration in cell viability, proliferation, migration, or other phenotypic feature can be correlated with efficacy of the agent. Telomerized cells can also be used in living wound models such as those described earlier, to screen the ability of other compounds to promote cell migration or the process of reepithelialization.
To determine the effect of telomerase on human keratinocytes, early passage (<PD5) cultures of both neonatal and adult keratinocytes were grown in an optimized medium and transfected with a vector encoding human telomerase reverse transcriptase (hTERT).
Human primary epidermal keratinocytes were obtained from Cascade Biologics (Portland, Oreg.). The cell lines are referred to in this disclosure according to their Cascade lot designation: HEKa18, HEKa2, HEKn9 and HEKn4 are two lines of adult keratinocytes and two lines of neonatal keratinocytes.
The cells were cultured in EpiLife™ serum-free medium plus calcium chloride at 0.06 mM and Human Keratinocyte Growth Supplement (HKGS) (Cascade Biologics, Portland, Oreg.). Cells were plated at 2-4×105 cells per T75 flask, refed every 2-3 days, and subcultured 4-7 days before high cell density was reached. PD (the number of population doublings) for every passage was calculated as log2 (number of cells at time of subculture/number of cells plated). Cumulative PD was plotted against time in culture so that replicative life span, senescence, slow growth or crisis, and immortalization could be assessed. Cells were considered to have been immortalized when the life span of a culture was greater than 50 PDs beyond that of parental cell line, and growth curves showed no sign of a decrease in proliferation rate.
Control HEKa and HEKn cultures senesced at PD 33-38 and PD51-56 respectively, as evidenced by complete cessation of cell division, senescence-associated (SA) β-galactosidase positive staining, and enlarged cellular morphology. In contrast, hTERT-transduced keratinocytes had indefinite lifespans and were negative for SA-β-galactosidase staining. Moreover, all hTERT-keratinocytes exhibited no slow phase growth or crisis stage, during which clonal populations with pRb/p16ink4a inactivation could have emerged
Total RNA was isolated from keratinocytes using High Pure™ RNA Isolation Kit (Roche). 100 ng total RNA was used for real time PCR quantitation of hTERT and hTR (the telomerase RNA component) with a light cycler (Roche). TeloTAGGG™ hTERT and hTR quantitation kits (Roche) and PCR were used according to the manufacturer's protocol. Telomerase activity was assessed by the PCR-based telomeric repeat amplification protocol (TRAP) assay (Kim et al., Nucl. Acids Res. 25:13, 1997). Mean telomere restriction fragment (TRF) lengths were determined by Southern blotting (Bodnar et al., Science 279:349, 1998).
Telomerase activity was quantitated using the formula
where TP is telomerase products from test sample, TP′ is products from heat-inactivated control, TI is internal control of sample, R8 is products from quantification standard, B is buffer blank, and RI is internal control of standard. The total product generated (TPG) is defined as 0.001 amol (600 molecules) of primer TS extended for at least three telomeric repeats by telomerase in the sample. One TPG corresponds roughly to the telomerase activity in one immortal cell. Values obtained are shown in Table 1:
Telomerase Activity in hTERT-Transduced Keratinocytes
The transduced keratinocytes expressed relatively high levels of hTERT transcripts that increased with passage, likely reflecting enrichment of telomerase-expressing cells (Panel A). This level of expression is roughly 100-200 fold greater than that seen in tumor cell lines such as H1299 and Raji. Expression of hTR (the RNA subunit of telomerase) was steady and similar between hTERT-keratinocytes and vector controls (data not shown). hTERT-keratinocytes had high levels of telomerase activity and elongated telomerase, while control keratinocytes were telomerase negative and telomerase progressively shortened with passage (Panels B & C).
pRb phosphorylation is required for progression through the S phase. pRb activity is regulated by proteins such as CDK4, cyclin D1 and p16 (Weinberg et al., Cell 81:323, 1995). To determine whether there were perturbations in the pRb/p16 pathway in hTERT-transduced keratinocytes, expression of pRb and p16 proteins was analyzed by Western blot analysis.
Western analysis for p16 (G175-1239, PharMingen), pRb (G3-245, PharMingen), p53 (OP29, Oncogene), cyclin D1 (G124-326, PharMingen), CDK4 (DCS-35, PharMingen), c-myc (N-262, Santa Cruz Biotechnology), GADD45 (H-165, Santa Cruz Biotechnology) and TFIIB (SC-225, Santa Cruz Biotechnology) was performed as described in Wang et al. (Nature 405:755, 2000). The antibody to pRb recognizes both hyper- and hypo-phosphorylated forms of the proteins (Jiang et al., Nature Genet 21:111, 1999).
(a) Vector control (BABE) and hTERT-expressing keratinocytes were maintained at either subconfluent cultures (S) or confluent cultures for 72 hours (C) and analyzed for pRb, p53, cyclin D1, CDK4, and TFIIB.
(b) Vector control and hTERT-expressing keratinocytes were analyzed for p16INK4a protein levels at early and late population doublings (PDs). (c) Vector control (B) and hTERT-keratinocytes at different PDs were analyzed for c-myc and GADD45 expression. TFIIB protein was used to normalize loading in panels (b) and (c).
It was found that pRb was predominantly hyperphosphorylated in subconfluent, proliferating keratinocytes, but was hypophosphorylated when the cells were maintained at confluence (Panel A). Levels of pRb were also down-regulated at confluence. Cyclin D1 and CDK4 were expressed at similar levels in proliferating hTERT-transduced and control keratinocytes, but cyclin D1 expression was down-regulated upon growth arrest (Panel a). The amount of p16 increased in late passage keratinocytes (Panel b). In contrast to previous reports, it was found that all hTERT-keratinocytes retained stable p16INK4a protein levels even after dramatic life span extension (Panel b).
p53 plays an important role in initiation of senescence-associated growth arrest (Sedivy et al., Proc. Natl. Acad. Sci. USA 95:9078, 1998). In these experiments, it was found that p53 was normally expressed in hTERT-transduced keratinocytes in both growing and non-growing states (Panel A). Thus, neither pRb/p16INK4a nor p53 inactivation are required for immortalization of human keratinocytes by telomerase.
Wang et al. (Nature 405:755, 2000) reported that hTERT-driven cell proliferation and immortalization are associated with activation of the c-myc protooncogene. This was after long-term culture of immortalized epithelial cells that had suffered previous inactivation of the pRb/p16INK4a pathway. However, it has now been discovered that hTERT-immortalized normal keratinocytes at both early and late passages, show that c-myc and GADD45 (a downstream target of c-myc) were expressed at levels similar to that seen in control populations (
Telomerase-transduced cultures were examined under conditions known to induce arrest and differentiation of young keratinocytes: high cell density, high calcium concentrations, EGF removal, TGF-β treatment, or exposure to phorbol ester.
Under these conditions, the fractions of cycling hTERT-keratinocytes were similar to that of control cells. In contrast, the SCC-4 human squamous cell carcinoma cell line was not dependent on EGF or inhibited by phorbol ester. These results indicate that hTERT-immortalized keratinocytes retain normal c-myc expression and growth regulatory mechanisms.
Human keratinocyte migration and proliferation are essential for re-epithelialization of skin wounds. In this experiment, the effect of replicative senescence and hTERT-transduction in a culture model of wound closure was examined.
Keratinocytes were plated at 1×105 cells/T25 flask. Once the cells reached 80-90% confluence, the monolayer of cells was scratched in a standardized manner with a plastic apparatus to create a cell-free zone approximately 1 mm across.
Retrovirus transduction for permanent expression was effected using the hTERT/BABE vector described in Example 1. When the keratinocytes were growing in log phase, the medium was replaced with 5 mL viral supernatant in DMEM/F12 medium at a titer of 3-5×106 mL−1. After culturing overnight at 37° C. in 5%CO2/95%, the cells were washed twice in PBS, and selected for 7 days in EpiLife™ medium containing 0.5 μg/mL puromycin, and then grown in regular EpiLife™ medium.
Adenovirus transduction was effecting using a replication-deficient (E1 and E3 deleted) adenovirus, containing an expression cassette in which the hTERT encoding region is under control of CAG (CMV enhancer, chicken β-actin promoter, and the rabbit β-globin polyadenylation signal). When the keratinocytes were ˜80-90% confluent, the well was scratched to create a cell-free zone, and simultaneously transduced with the adenovirus vector at 2-10 MOI in EpiLife™ medium (1 MOI≡1 PFU≡0.7 TCID). The cells were cultured overnight at 37° C. in 5%CO2/95%, washed twice in PBS, and then grown in regular EpiLife™ medium.
In vitro re-epithelialization or wound closure was documented by photography through a 40×objective over a 1-4 day period. The width of the wound was measured at three different places in each of three replicate plates, and the rate of wound closure was calculated by linear regression of the mean wound width as a function of time.
To test whether telomerase could rescue age-associated deficits in wound closure in this model system, late-passage cultures of keratinocytes were wounded and then transduced with adenoviral vector for transient hTERT expression (AdhTERT). The identical adenovirus containing GFP in place of hTERT was used as a control.
Cells transduced with the hTERT retrovirus were measured for their resistance to apoptotic cell death, induced by TNF-α or UV irradiation.
Apoptosis is characterized in the early stages by translocation of membrane phosphatidylserine (PS) from the inner to the outer leaflet of the plasma membrane. Annexin V is a 35-36 kDa calcium-dependent binding protein with a high affinity for PS, which can be used to stain for externalized PS in early apoptosis.
For TNF-α induced apoptosis, keratinocytes were transduced with hTERT retrovirus or BABE control. The transduced cells were then cultured for 48 hours in standard keratinocyte culture medium, or medium containing TNF-α. The cells were washed in PBS containing 0.5% BSA (or 1% FBS). 5×105 cells were combined with 0.5 mL 1×Binding Buffer from the Annexin V FITC Kit. 5 μL Annexin V FITC and 10 μL propidium iodide were added, and the mixture was incubated at room temperature in the dark for 10 min. They were then measured for percentage positive cells and mean fluorescence intensity by flow cytometry.
For apoptosis induced by UV irradiation, primary adult keratinocytes were seeded in 100 mm TC dishes at 3×105 per dish, and cultured in EpiLife® medium. Cells reached about 40% confluence at 3 days, and were transduced in fresh medium containing AdhTERT at 10 MOI. AdhTERT is a replication-deficient, E1 and E3 regions deleted, adenovirus containing a cassette encoding the human telomerase gene under the control of CAG (comprising the CMV enhancer, chicken actin promoter, and a portion of 3′ untranslated region containing the polyadenylation site of rabbit globin gene). After culturing with AdhTERT for 72 h, the cells were washed twice with Ca++- and Mg++-free PBS. UV irradiation was performed for 24 h, and the cells were then stained with Annexin V.
The results show that the protective effects of hTERT extend to the progeny of the cells transfected on day 8. Since adenovirus vectors provide only transient expression, the long-lasting effect may ensue from the lengthening of telomerase caused by hTERT in the parent cells.
In the previous examples, telomerase expression was shown to increase replicative capacity of keratinocytes, render them less susceptible to apoptosis, and increase their capacity to re-epithelialize a wound. In this experiment, the wound healing effect was decoupled from the proliferation effect, showing that wound closure is not due simply to an increase in cell replication.
Keratinocyte cell lines were plated at 1×105 per T25 flask. Once they had grown to 80-90% confluence (˜5×105), the cell monolayer was scratched as before to create a cell-free zone. The cells were treated with mitomycin c at 10 μg/mL for 2 hours. The medium was then aspirated and replaced with fresh EpiLife™ medium, with or without Adeno-hTERT or Adeno-GFP (control), to transiently increase telomerase expression. After transducing overnight, the medium was replaced with fresh medium, and the rate of wound closure was measured for 4 days in triplicate.
A summary of the kinetics of epithelial cell migration is shown in Table 2.
Kinetics of Wound Closure
(hours to achieve 50%
HEKn9 pBABE PD8
33.0 ± 1.2
HEKn9 pBABE PD41
113.4 ± 5.7
HEKn9 PD42 + AdGFP
108.9 ± 17.7
HEKn9 PD42 + AdGFP + Mitomycin c
189.2 ± 28.9
HEKn9 pBABE/TERT PD152
31.6 ± 0.8
HEKn9 PD42 + AdhTERT
34.3 ± 2.3
HEKn9 PD42 + AdhTERT + Mitomycin c
40.3 ± 2.1
pBABE = retrovirus control
pBABE/TERT = retroviral vector for expressing TERT
AdGFP = adenoviral vector for expressing GFP (control)
AdhTERT = adenoviral vector for expressing TERT
In conclusion, it has been found that hTERT-treated keratinocytes have increased replicative capacity, and are resistant to apoptosis. They retain normal growth control, as shown by dependence on epidermal growth factor (EGF) and sensitivity to phorbol ester (TPA). hTERT-treated keratinocytes do not spontaneously activate c-myc, and retain functional p53 and pRB/p16ink4a cell cycle checkpoint. Both stable and transient hTERT expression increases migration and accelerates wound healing in aging keratinocytes.
In this study, it was shown that AdhTERT gene delivery induces a specific and robust enhancement of granulation tissue formation in the ischemic ear wounds of aged rabbits.
The adenovirus vector encoding hTERT under control of the CAG expression system was described in Example 4. Rabbit fibroblasts were obtained from ATCC (CRL-1414), grown in BME +10% FBS to passage 33, infected with AdhTERT or Ad-null for 24 hr at different MOI, and analyzed 48 hrs later for telomerase activity using the TRAP assay. Skin tissues were obtained from young rabbits and maintained in DMEM +10% FBS ex vivo. The tissues were injected intradermally with 2×109 viral particles and harvested 3 days later. Frozen tissue sections were analyzed for hTERT expression using anti-hTERT antibody as described below.
Ear wounds were induced in rabbits as an established clinically relevant model for wound ischemia (Ahn, S. T. & T. A. Mustoe, Ann Plast Surg 24:17, 1990; Wu et al., Am J Pathol 154:301, 1999). New Zealand white rabbits (>55 months of age) were prepared by shaving the ears and prepping with betadine solution. An incision was made to the level of bare cartilage at the base of each ear. Both ears of each rabbit were made ischemic by dissecting the rostral and central arteries, with preservation of the caudal, central and rostral veins. The incision was closed with a running 4-0 Vicryl™ suture. Three to five full thickness (6 mm) circular wounds were then made on the inner surface of the ear down to bare cartilage.
Adenoviral gene transfection was performed by delivering 2×109 viral particles of AdhTERT or Ad-null (control) per ear wound. Two thirds of total dose was injected at 4 periwound locations at 5 μL each, using a Hamilton syringe with a 30 gauge needle. One third of the dose was topically placed within the defect in 10 μL. Sterile Tegaderm™ dressing (3M Health Care, St. Paul, Minn.) was placed over each wound upon completion of the procedure. The dressings were changed as needed over the next 12 days, at which time the animals were sacrificed and the wounds harvested for histological and biochemical analysis.
Telomerase activity was measured according to standard TRAP assay procedures described earlier, as applied to frozen skin tissue homogenized in lysis buffer.
Immunohistochemical analysis of hTERT expression was performed on 6 μm frozen tissue sections fixed in 4% paraformaldehyde in PBS (pH 7), rinsed in PBS and permeabilized in PBS containing 0.1% Triton™ X-100. The sections were blocked in 5% goat serum in PBS for 30 min at room temp, drained and incubated with anti-hTERT antibody (1A4, 2.5 μg/ml) for 1 h. After washing several times in PBS, Texas-Red™ conjugated goat anti-mouse IgG (Jackson Immunolabs, Westgrove, Pa.) was added at 7.5 μg/mL for 30 min at room temp in the dark. The sections were then washed again with PBS, mounted using Vectashield™ mounting medium containing DAPI (Vector Labs), and viewed under a Nikon fluorescent microscope.
Data were collected from histological sections to determine the extent of wound re-epithelialization and new granulation tissue formation. The wound healing parameters were measured twice using a calibrated reticle from H&E-stained paraffin tissue sections by observers blinded to treatment. Analysis of all wound parameters was performed by Student's t-test and analysis of variance with post hoc analysis using Tukey's standardized range. All comparisons were made to paired wounds. Any dependent associations were analyzed using Spearman's correlation of coefficients.
To determine if hTERT expression in rabbit skin can enhance wound healing, AdhTERT or Ad-null was administered to ischemic ear wounds of aged rabbits by both intradermal injection and topical application. Pilot experiments using young rabbits showed that AdhTERT causes hTERT expression in the dermal regions 3 days after wounding and virus administration . Analysis of the aged wounds at day 12 also showed hTERT positive dermal cells, albeit at less frequency, probably due to the transient nature of adenoviral gene expression.
Histological analysis of aged rabbit isohemic ear wounds
(day 12 post-wounding)
(n = 5)
(n = 15)
(n = 9)
Area (×104 μm2)
5 ± 1
7 ± 2
27 ± 6*
340 ± 5
445 ± 45
986 ± 152*
Peak to peak distance (μm)
5245 ± 180
5048 ± 102
3890 ± 330*
Peak height (μm)
335 ± 28
312 ± 27
407 ± 20
Epithelial gap (μm)
2750 ± 822
1529 ± 468
1167 ± 519
Epithelial height (μm)
145 ± 23
124 ± 14
130 ± 18
*p < 0.01 between Ad-null and AdhTERT
The results show that transient expression of hTERT can specifically enhance new granulation tissue formation, which is critical in effecting wound healing. The lack of observable effect on epithelial growth or migration is most likely due to the inefficient gene delivery to the epithelium.
The hTERT effect on granulation tissue formation is quite dramatic, despite the relative inefficient gene transfer to the skin. This suggests that in addition to influencing the phenotype and/or replicative capacity of the transduced cells, hTERT expression cells may indirectly influence the phenotype of neighboring cells—for example, by elaborating trans-acting factors or altering the extra-cellular matrix environment. There was no abnormal inflammatory response in the hTERT treated wounds beyond that observed with normal wound healing, suggesting that local AdhTERT gene delivery can be used safely.
The ability of hTERT gene to reconstitute function in rhesus monkey cells was demonstrated by positive hTERT protein expression and telomerase activity following AdhTERT transduction of rhesus monkey fibroblasts in culture.
The results show that monkey skin fibroblasts do not express detectable endogenous telomerase activity. The weak signals in the heat inactivated lanes are likely to be due to leakage from other adjacent lanes. Upon transduction with AdhTERT but not Ad-null, telomerase activity was reconstituted and the level of telomerase activity showed a dose related increase with the transducing viral dose. Immunocytochemical analysis also revealed hTERT positive cells in AdhTERT transduced rhesus monkey fibroblast cultures.
Wound healing experiments were conducted using an established model in aged rhesus monkeys (Roth et al., J Gerontol A Biol. Sci. Med. Sci. 52:B98-102, 1997). Full thickness wounds were created in female rhesus monkey monkeys (18-32 years old) anesthetized with ketamine (15 mg/kg) and diazepam (1 mg/kg). Four separate 5 mm punch biopsy wounds were made on the dorsal side of the animals. AdhTERT or Ad-null virus was applied at 1010 viral particles per wound to two wounds at the time of wounding. To measure wound closure, each monkey served as its own control. AdhTERT was used to treat 2 of the wounds on each animal, and Ad-null was administered to the other 2 wounds. Two thirds of each dose was delivered around the wound edge by 8 intra-dermal injections of 5 μL using a Hamilton syringe with a 30 gauge needle. The remaining third of the viral dose was applied topically into the wound defect (20 μL). The percentage of wound area remaining was assessed every other day. Wound tracings were performed using a single-layer plastic film placed over the biopsy site and % wound area remaining was quantified as number of pixels using NIH Image analysis software. Upon complete healing, an 8 mm punch biopsy was collected around each wound and processed for histological and biochemical analysis.
The AdhTERT vector was found to cause hTERT expression in the dermal regions 3 days after wounding and virus administration.
Chronic ulcers are characterized by impaired wound healing and frequently repeated wounding at the same sites. They may be partially due to the compromised regenerative capacity of skin cells as a consequence of replicative senescence. In addition, the aberrant gene expression/phenotype often associated with the state of senescence may further exacerbate the pathology found in chronic wounds.
To extend the other findings provided in this disclosure, an assay of ex-vivo epidermal migration was developed using intact human skin tissues. The tissue was obtained from both normal donors and from donors with chronic wounds, and was used to determine the effect of hTERT gene expression on epidermal migration.
Human skin tissues from autopsy or surgical procedures were provided by Research Tissue Recovery Network (Blue Springs, Mo.) and by Dr. Spencer Brown at University of Texas Southwestern Medical Center (Dallas, Tex.) within 24 hr of isolation. Normal skin tissues were obtained from donors without any wounds or from anatomical sites distal from any affected wounds; wound tissues were obtained from sites close to or at the edges of affected acute or chronic wounds.
Upon receipt, skin tissues were trimmed of subcutaneous fat and washed 5 times using DMEM supplemented with streptomycin (10 μg/mL) and penicillin (10 units/mL). Generally, 4 or 6 mm full thickness punches were made from the skin samples using a sterile biopsy (uni-punch, Premier Medical Products, King of Prussia, Pa.). The skin punches were attached to the bottom of Petri dishes or 6-well tissue culture plates using skin closure glue Nexabond™ (Veterinary Products Laboratories, Phoenix, Ariz.), submerged in DMEM supplemented with 10% FBS and Pen/Strep, and incubated at 37° C. with 5% CO2 for up to 7 days. For each time point, 3 skin punches were harvested and fixed in 10% neutral buffered formalin for 24 h. The tissues were paraffin embedded on edge and 6 micron serial sections were generated. For each skin punch, 3 sections at different depths were stained with H&E and examined under a microscope. Photomicrographs of the sections were taken under a 2.5× object lens and the images saved as JPG files. To cover the entire tissue section, sometimes two overlapping photomicrographs were taken and assembled using Adobe PhotoShop® software.
Upper panels show hTERT staining; lower panels show co-localization with propidium iodide. Administration by injection caused hTERT expression to be mostly localized along the injection path. Bathing with AdhTERT (10 8 pfu/mL for 24 h) was less efficient in transducing the dermal cells, although a few cells lining the migrating epidermis did show hTERT expression.
To assess the effect of hTERT on epidermal migration, skin punches were treated with AdhTERT by direct injection or bathing. Results were compared with punches exposed to adenovirus encoding LacZ, adenovirus control (Ad-null), or no virus. One sample of the four tested (GTS 1384, age 78, normal skin) showed significant enhancement (
These results show that hTERT preferentially affects dermal tissues (normal or pathologic) that have sub-optimal epidermal migration. hTERT transduction is not mitogenic, nor does it significantly change the phenotype of young cells. But in older cells, hTERT enables the cells to proliferate further, and causes beneficial (“youthful”) changes that result in enhanced migration and epithelializing potential. Even a few hTERT expressing cells can rescue the senescent phenotype and generate growth factors or extracellular matrix components that improve epidermal cell migration over the wound surface.
The compositions and procedures described in this disclosure can be effectively modified by routine optimization without departing from the spirit of the invention embodied in the claims that follow.
Sequences Listed in this Disclosure
Homo sapiens telomerase
GenBank Locus NM 003210.
reverse transcriptase (TERT)
See also Nakamura et al.,
Science 277:955, 1997; and
GenBank Locus AF015950
Homo sapiens telomerase
GenBank Locus NM 0032107.
reverse transcriptase (TERT)
amino acid sequence
SEQ. ID NO: 1
gcagcgctgc gtcctgctgc gcacgtggga agccctggcc ccggccaccc ccgcgatgcc
gcgcgctccc cgctgccgag ccgtgcgctc cctgctgcgc agccactacc gcgaggtgct
gccgctggcc acgttcgtgc ggcgcctggg gccccagggc tggcggctgg tgcagcgcgg
ggacccggcg gctttccgcg cgctggtggc ccagtgcctg gtgtgcgtgc cctgggacgc
acggccgccc cccgccgccc cctccttccg ccaggtgtcc tgcctgaagg agctggtggc
ccgagtgctg cagaggctgt gcgagcgcgg cgcgaagaac gtgctggcct tcggcttcgc
gctgctggac ggggcccgcg ggggcccccc cgaggccttc accaccagcg tgcgcagcta
cctgcccaac acggtgaccg acgcactgcg ggggagcggg gcgtgggggc tgctgctgcg
ccgcgtgggc gacgacgtgc tggttcacct gctggcacgc tgcgcgctct ttgtgctggt
ggctcccagc tgcgcctacc aggtgtgcgg gccgccgctg taccagctcg gcgctgccac
tcaggcccgg cccccgccac acgctagtgg accccgaagg cgtctgggat gcgaacgggc
ctggaaccat agcgtcaggg aggccggggt ccccctgggc ctgccagccc cgggtgcgag
gaggcgcggg ggcagtgcca gccgaagtct gccgttgccc aagaggccca ggcgtggcgc
tgcccctgag ccggagcgga cgcccgttgg gcaggggtcc tgggcccacc cgggcaggac
gcgtggaccg agtgaccgtg gtttctgtgt ggtgtcacct gccagacccg ccgaagaagc
cacctctttg gagggtgcgc tctctggcac gcgccactcc cacccatccg tgggccgcca
gcaccacgcg ggccccccat ccacatcgcg gccaccacgt ccctgggaca cgccttgtcc
cccggtgtac gccgagacca agcacttcct ctactcctca ggcgacaagg agcagctgcg
gccctccttc ctactcagct ctctgaggcc cagcctgact ggcgctcgga ggctcgtgga
gaccatcttt ctgggttcca ggccctggat gccagggact ccccgcaggt tgccccgcct
gccccagcgc tactggcaaa tgcggcccct gtttctggag ctgcttggga accacgcgca
gtgcccctac ggggtgctcc tcaagacgca ctgcccgctg cgagctgcgg tcaccccagc
agccggtgtc tgtgcccggg agaagcccca gggctctgtg gcggcccccg aggaggagga
cacagacccc cgtcgcctgg tgcagctgct ccgccagcac agcagcccct ggcaggtgta
cggcttcgtg cgggcctgcc tgcgccggct ggtgccccca ggcctctggg gctccaggca
caacgaacgc cgcttcctca ggaacaccaa gaagttcatc tccctgggga agcatgccaa
gctctcgctg caggagctga cgtggaagat gagcgtgcgg gactgcgctt ggctgcgcag
gagcccaggg gttggctgtg ttccggccgc agagcaccgt ctgcgtgagg agatcctggc
caagttcctg cactggctga tgagtgtgta cgtcgtcgag ctgctcaggt ctttctttta
tgtcacggag accacgtttc aaaagaacag gctctttttc taccggaaga gtgtctggag
caagttgcaa agcattggaa tcagacagca cttgaagagg gtgcagctgc gggagctgtc
ggaagcagag gtcaggcagc atcgggaagc caggcccgcc ctgctgacgt ccagactccg
cttcatcccc aagcctgacg ggctgcggcc gattgtgaac atggactacg tcgtgggagc
cagaacgttc cgcagagaaa agagggccga gcgtctcacc tcgagggtga aggcactgtt
cagcgtgctc aactacgagc gggcgcggcg ccccggcctc ctgggcgcct ctgtgctggg
cctggacgat atccacaggg cctggcgcac cttcgtgctg cgtgtgcggg cccaggaccc
gccgcctgag ctgtactttg tcaaggtgga tgtgacgggc gcgtacgaca ccatccccca
ggacaggctc acggaggtca tcgccagcat catcaaaccc cagaacacgt actgcgtgcg
tcggtatgcc gtggtccaga aggccgccca tgggcacgtc cgcaaggcct tcaagagcca
cgtctctacc ttgacagacc tccagccgta catgcgacag ttcgtggctc acctgcagga
gaccagcccg ctgagggatg ccgtcgtcat cgagcagagc tcctccctga atgaggccag
cagtggcctc ttcgacgtct tcctacgctt catgtgccac cacgccgtgc gcatcagggg
caagtcctac gtccagtgcc aggggatccc gcagggctcc atcctctcca cgctgctctg
cagcctgtgc tacggcgaca tggagaacaa gctgtttgcg gggattcggc gggacgggct
gctcctgcgt ttggtggatg atttcttgtt ggtgacacct cacctcaccc acgcgaaaac
cttcctcagg accctggtcc gaggtgtccc tgagtatggc tgcgtggtga acttgcggaa
gacagtggtg aacttccctg tagaagacga ggccctgggt ggcacggctt ttgttcagat
gccggcccac ggcctattcc cctggtgcgg cctgctgctg gatacccgga ccctggaggt
gcagagcgac tactccagct atgcccggac ctccatcaga gccagtctca ccttcaaccg
cggcttcaag gctgggagga acatgcgtcg caaactcttt ggggtcttgc ggctgaagtg
tcacagcctg tttctggatt tgcaggtgaa cagcctccag acggtgtgca ccaacatcta
caagatcctc ctgctgcagg cgtacaggtt tcacgcatgt gtgctgcagc tcccatttca
tcagcaagtt tggaagaacc ccacattttt cctgcgcgtc atctctgaca cggcctccct
ctgctactcc atcctgaaag ccaagaacgc agggatgtcg ctgggggcca agggcgccgc
cggccctctg ccctccgagg ccgtgcagtg gctgtgccac caagcattcc tgctcaagct
gactcgacac cgtgtcacct acgtgccact cctggggtca ctcaggacag cccagacgca
gctgagtcgg aagctcccgg ggacgacgct gactgccctg gaggccgcag ccaacccggc
actgccctca gacttcaaga ccatcctgga ctgatggcca cccgcccaca gccaggccga
gagcagacac cagcagccct gtcacgccgg gctctacgtc ccagggaggg aggggcggcc
cacacccagg cccgcaccgc tgggagtctg aggcctgagt gagtgtttgg ccgaggcctg
catgtccggc tgaaggctga gtgtccggct gaggcctgag cgagtgtcca gccaagggct
gagtgtccag cacacctgcc gtcttcactt ccccacaggc tggcgctcgg ctccacccca
gggccagctt ttcctcacca ggagcccggc ttccactccc cacataggaa tagtccatcc
ccagattcgc cattgttcac ccctcgccct gccctccttt gccttccacc cccaccatcc
aggtggagac cctgagaagg accctgggag ctctgggaat ttggagtgac caaaggtgtg
ccctgtacac aggcgaggac cctgcacctg gatgggggtc cctgtgggtc aaattggggg
gaggtgctgt gggagtaaaa tactgaatat atgagttttt cagttttgaa aaaaa
SEQ. ID NO: 2
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US4016036||Nov 14, 1975||Apr 5, 1977||Massachusetts Institute Of Technology||Process for serially culturing keratinocytes|
|US4304866||Nov 14, 1979||Dec 8, 1981||Massachusetts Institute Of Technology||Transplantable sheets of living keratinous tissue|
|US4745098||Feb 24, 1984||May 17, 1988||The Regents Of The University Of California||Compositions and method for improving wound healing|
|US4837024||May 13, 1988||Jun 6, 1989||The Regents Of The University Of California||Compositions, articles and mehtod for improving wound healing|
|US5556620||Mar 31, 1994||Sep 17, 1996||Cetus Oncology Corporation||Use of recombinant colony stimulating factor-1 to enhance wound healing|
|US5561107||Apr 20, 1994||Oct 1, 1996||Demeter Biotechnologies, Ltd.||Method of enhancing wound healing by stimulating fibroblast and keratinocyte growth in vivo, utilizing amphipathic peptides|
|US5580781||Apr 6, 1995||Dec 3, 1996||Advanced Tissue Sciences, Inc.||Three-dimensional tumor cell and tissue culture system|
|US5583016||Oct 27, 1994||Dec 10, 1996||Geron Corporation||Mammalian telomerase|
|US5641670||May 13, 1994||Jun 24, 1997||Transkaryotic Therapies, Inc.||Protein production and protein delivery|
|US5698436||Jun 6, 1995||Dec 16, 1997||Whitehead Institute For Biomedical Research||Introduction and expression of foreign genetic material in epithelial cells|
|US5718897||Dec 31, 1996||Feb 17, 1998||Trustees Of Tufts College||Enhancing keratinocyte migration and proliferation|
|US5720981||Nov 14, 1994||Feb 24, 1998||Sloan-Kettering Institute For Cancer Research||Epidermal cell extracts and method to enhance wound healing and regenerate epidermis|
|US5733761||May 26, 1995||Mar 31, 1998||Transkaryotic Therapies, Inc.||Protein production and protein delivery|
|US5824647||Jun 1, 1995||Oct 20, 1998||Postlethwaite; Arnold E.||Chemotactic wound healing peptides|
|US5861153||Jan 23, 1997||Jan 19, 1999||Societe L'oreal S.A.||Skin equivalent comprising langerhans' cells|
|US5965530||Jun 6, 1995||Oct 12, 1999||Amgen Inc.||Therapeutic uses of keratinocyte growth factor|
|US5980888||Oct 24, 1995||Nov 9, 1999||Roche Diagnostics Gmbh||Keratinocytes attached to microcarriers for treatment of skin wounds|
|US5997863||Jul 8, 1994||Dec 7, 1999||Ibex Technologies R And D, Inc.||Attenuation of wound healing processes|
|US6025150||Nov 18, 1997||Feb 15, 2000||The Regents Of The University Of Michigan||Methods and compositions for wound healing|
|US6077602||Mar 21, 1996||Jun 20, 2000||Mobil Oil Corporation||Heat sealable film|
|US6110208||Apr 25, 1996||Aug 29, 2000||Fidia Advanced Biopolymers S.R.L||Artificial skin containing as support biocompatible materials based on hyaluronic acid derivatives|
|US6166178||Nov 19, 1997||Dec 26, 2000||University Technology Corporation||Telomerase catalytic subunit|
|US6191110||Jan 19, 1999||Feb 20, 2001||Demegen, Inc.||Method of enhancing wound healing by stimulating fibroblast and keratinocyte growth in vivo, utilizing amphipathic peptides|
|US6261556||Oct 18, 1999||Jul 17, 2001||Geron Corporation||Purified telomerose|
|US6261836||May 9, 1997||Jul 17, 2001||Geron Corporation||Telomerase|
|US6617110||Nov 22, 2000||Sep 9, 2003||Geron Corporation||Cells immortalized with telomerase reverse transcriptase for use in drug screening|
|WO1997008295A1||Aug 22, 1996||Mar 6, 1997||Lifecell Corporation||Reconstituted skin|
|WO1997023602A1||Dec 19, 1996||Jul 3, 1997||Societe Des Produits Nestle S.A.||Improved immortalized human skin cell lines and novel serum-free medium useful for the production thereof|
|WO1999027113A1||Nov 25, 1998||Jun 3, 1999||Geron Corporation||Mouse telomerase reverse transcriptase|
|WO1999047644A1||Mar 18, 1999||Sep 23, 1999||Peter Maccallum Cancer Institute||Keratinocyte stem cells|
|WO1999054435A2||Apr 7, 1999||Oct 28, 1999||Societe Des Produits Nestle||Immortalised cell lines derived from normal human skin tissues|
|WO2000031238A2||Nov 24, 1999||Jun 2, 2000||Genetica, Inc.||Methods and reagents for increasing proliferative capacity and preventing replicative senescence|
|WO2000047148A1||Feb 9, 2000||Aug 17, 2000||The Research Foundation Of State University Of New York||Methods and compositions for enhancing fibroblast migration|
|1||Bodnar, et al., Extension of life-span by introduction of telomerase into normal human cells, Science 279:349 (1998).|
|2||Campisi, et al., The role of cellular senescence in skin aging, J Investig Dermatol Symp Proc. 3:1 (1998).|
|3||Deveci, M., Telomeres and telomerase and their possible future in plastic surgery, Plast. Reconstr. Surg. 104:1588 (1999).|
|4||Dickson, et al., Human keratinocytes that express hTERT and also bypass a p16(INK4a)-enforced mechanism that limits life span become immortal yet retain normal growth and differentiation charachteristics, Mol. Cell. Biol. 20:1436 (2000).|
|5||Driscoll, et al., Telomerase in alveolar epithelial development and repair, Am J. Physiol. Lung. Cell. Mol. Physiol. 279:L1191 (2000).|
|6||Farwell, et al., Genetic and epigenetic changes in human epithelial cells immortalized by telomerase, Am. J. Pathol. 156:1537 (2000).|
|7||Fujimoto, et al., Expression of telomerase components in oral keratinocytes and squamous cell carcinomas, Oral. Oncol. 37:132 (2001).|
|8||Funk, et al., Telomerase expression restores dermal integrity to in vitro-aged fibroblasts in a reconstituted skin model, Exp. Cell Res. 258:270 (2000).|
|9||Gonzalez-Suarez, et al., Increased epidermal tumors and increased skin wound healing in transgenic mice overexpressing the catalytic subunit of telomerase, mTERT, in basal keratinocytes, EMBO J 20:2619 (2001).|
|10||Harle-Bachor, et al., Telomerase activity in the regenerative basal layer of the epidermis in human skin and in immortal and carcinoma-derived skin keratinocytes, Proc. Natl. Acad. Sci. USA 93:6476 (1996).|
|11||Holmberg, et al., Ester synthesis with dicyclohexylcarbodiimide improved by acid catalysts, Acta Chemica Scandinavica B 33:410 (1979).|
|12||Jiang, et al., Telomerase expression in human somatic cells does not induce changes associated with a transformed phenotype, Nat. Genet. 21:111 (1999).|
|13||Kang, et al., Replicative senescence of normal human oral keratinocytes is associated with the loss of telomerase activity without shortening of telomeres, Cell Growth Differ. 9:85 (1998).|
|14||Kiyono, et al., Both Rb/p16<SUP>INK4a </SUP>inactivation and telomerase activity are required to immortalize human epithelial cells, Nature 396:84 (1998).|
|15||LaFrance, et al., Novel living skin replacement biotherapy approach for wounded skin tissues, Tissue Eng 5:153 (1999).|
|16||Li, et al., Identification and isolation of candidate human keratinocyte stem cells based on cell surface phenotype, Proc Natl Acad Sci USA 95:3902 (1998).|
|17||Martin, Wound healing-aiming for perfect skin regeneration, Science 276:75 (1997).|
|18||Matsui, et al., Influence of aging and cell senescence on telomerase activity in keratinocytes, J. Dermatol. Sci. 22:80 (2000).|
|19||Mattson, et al., Emerging roles for telomerase in neuronal development and apoptosis, J. Neurosci Res 63:1 (2001).|
|20||Mendez, et al., Fibroblasts cultured from venous ulcers display cellular characteristics of senescence, J. Vasc. Surg. 28:876 (1998).|
|21||Morales, et al., Lack of cancer-associated changes in human fibroblasts after immortalization with telomerase, Nature Genet. 21:115 (1999).|
|22||Nakamura, et al., Telomerase Catalytic Subunit Homologs from Fission Yeast and Human, Science 277:955 (1997).|
|23||Ogoshi, et al., In situ hybridization analysis of the expression of human telomerase RNA in normal and pathologic conditions of the skin, J. Invest. Dermatol. 110:818 (1998).|
|24||Osanai, et al., Transcient increase in telomerase activity of proliferating fibroblasts and endothelial cells in granulation tissue of the human skin, Wound Repair Regen. 10:59 (2002).|
|25||Rambatla, et al., In vitro differentiation capacity of telomerase immortalized human RPE cells, invest Ophthalmol. Vis. Sci. 43:1622 (2002).|
|26||Ramirez, et al., Progressive Increase in Telomerase Activity From Benign Melanocytic Conditions to Malignant Melanoma, Neoplasia 1:00 (1999).|
|27||Ramirez, et al., Putative telomere-indepentant mechanisms of replicative aging reflect inadequate growth conditions, Genes & Dev. 15:398 (2001).|
|28||Ramirez, et al., Telomerase activity concentrates in the mitotically active segments of human hair follicles, J. Invest. Dermatol. 108:113 (1997).|
|29||Rudolph, et al., Longevity, stress response, and cancer in aging telomerase-deficient mice, Cell 96:701 (1999).|
|30||Taylor, et al., Detection of Telomerase Activtion in Malignant and Nonmalignant Skin Conditions, J. Invest. Dermatol. 106:759 (1996).|
|31||Ueda, et al., Evidence for UV-associated Activation of Telomerase in Human Skin, Cancer Research 57:370 (1999).|
|32||Voigt, et al., Cultured epidermal keratinocytes on a microspherical transport system are feasible to reconstitute the epidermis in full-thickness wounds, Tissue Eng. 5:563 (1999).|
|33||Wang, et al., Risky immortalization by telomerase, Nature 405:755 (2000).|
|34||Yang, et al., Human endothelial cell life-extension by telomerase expression, J. Biol. Chem. 274:26141 (1999).|
|35||Yang, et al., Telomerized human microvasculature is functional in vivo, Nat. Biotechnol. 19:219 (2001).|
|36||Zhao, P., et al., Telomerase activity in radiation-induced chronic human skin ulcers, J. Environ. Pathol. Toxicol. Oncol. 18:17 (1999).|
|37||Zhou, et al., Expression of telomerase reverse transcriptase in radiation-induced chronic human skin ulcer, J. Environ. Pathol. Toxicol. Oncol. 21:67 (2002).|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7413864||Jun 24, 2004||Aug 19, 2008||Geron Corporation||Treating cancer using a telomerase vaccine|
|US7517971||Nov 22, 2000||Apr 14, 2009||Geron Corporation||Muteins of human telomerase reverse transcriptase lacking telomerase catalytic activity|
|US7560437||Jul 14, 2009||Geron Corporation||Nucleic acid compositions for eliciting an immune response against telomerase reverse transcriptase|
|US7585622||Nov 2, 1999||Sep 8, 2009||Geron Corporation||Increasing the proliferative capacity of cells using telomerase reverse transcriptase|
|US7622549||Jun 24, 2004||Nov 24, 2009||Geron Corporation||Human telomerase reverse transcriptase polypeptides|
|US7750121||Aug 17, 2005||Jul 6, 2010||Geron Corporation||Antibody to telomerase reverse transcriptive|
|US8222392||Aug 20, 2007||Jul 17, 2012||Geron Corporation||Kit for detection of telomerase reverse transcriptase nucleic acids|
|US8236774||Aug 7, 2012||Geron Corporation||Human telomerase catalytic subunit|
|US8709995||Aug 20, 2007||Apr 29, 2014||Geron Corporation||Method for eliciting an immune response to human telomerase reverse transcriptase|
|US8796438||Aug 14, 2006||Aug 5, 2014||Geron Corporation||Nucleic acids encoding inactive variants of human telomerase|
|US9226737||Feb 3, 2012||Jan 5, 2016||University Of Massachusetts||Negative pressure wound closure device|
|US9301742||Dec 23, 2014||Apr 5, 2016||University Of Massachusetts||Negative pressure wound closure device|
|US20030096344 *||Jan 11, 2002||May 22, 2003||Cech Thomas R.||Human telomerase catalytic subunit: diagnostic and therapeutic methods|
|US20040242529 *||Jun 24, 2004||Dec 2, 2004||Geron Corporation||Vector encoding inactivated telomerase for treating cancer|
|US20040247613 *||Jun 24, 2004||Dec 9, 2004||Geron Corporation||Treating cancer using a telomerase vaccine|
|US20060040307 *||Aug 17, 2005||Feb 23, 2006||Geron Corporation||Human telomerase catalytic subunit|
|US20060275267 *||Aug 14, 2006||Dec 7, 2006||Morin Gregg B||Nucleic acids encoding inactive variants of human telomerase|
|US20080279871 *||Aug 20, 2007||Nov 13, 2008||Geron Corporation||Immunogenic composition|
|US20090269739 *||Aug 20, 2007||Oct 29, 2009||Geron Corporation||Kit for detection of telomerase reverse transcriptase nucleic acids|
|U.S. Classification||514/44.00R, 424/93.1|
|International Classification||A61K38/45, A61L26/00, A61K48/00, A61K35/36, A61L15/44, A61L27/38, A61K35/12, A61L15/40, C12N5/071|
|Cooperative Classification||A61K38/45, A61L26/0066, C12N2799/022, A61L27/3804, A61L2300/258, C12N2799/027, C12N2510/04, A61L15/44, A61L2300/412, A61K35/12, A61K35/36, A61L27/3813, A61L15/40, C12N5/0629|
|European Classification||A61L27/38B4, A61L27/38B, C12N5/06B9K, A61K38/45, A61L26/00H2, A61K35/36, A61L15/44, A61L15/40|
|Oct 7, 2002||AS||Assignment|
Owner name: GERON CORPORATION, CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:JIANG, XU-RONG;CHIU, CHOY-PIK;HARLEY, CALVIN B.;REEL/FRAME:013156/0936;SIGNING DATES FROM 20020903 TO 20020906
|Jan 26, 2011||FPAY||Fee payment|
Year of fee payment: 4
|Feb 11, 2015||FPAY||Fee payment|
Year of fee payment: 8